Статті в журналах з теми "Carbocyclic compounds"
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Murarka, Sandip, and Andrey Antonchick. "Metal-Catalyzed Oxidative Coupling of Ketones and Ketone Enolates." Synthesis 50, no. 11 (May 3, 2018): 2150–62. http://dx.doi.org/10.1055/s-0037-1609715.
Повний текст джерелаSidi Mohamed, Bemba, Christian Périgaud, and Christophe Mathé. "Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues." Beilstein Journal of Organic Chemistry 13 (February 9, 2017): 251–56. http://dx.doi.org/10.3762/bjoc.13.28.
Повний текст джерелаBiteau, Nicolas G., Sarah A. Amichai, Niloufar Azadi, Ramyani De, Jessica Downs-Bowen, Julia C. Lecher, Tamara MacBrayer, Raymond F. Schinazi, and Franck Amblard. "Synthesis of 4′-Substituted Carbocyclic Uracil Derivatives and Their Monophosphate Prodrugs as Potential Antiviral Agents." Viruses 15, no. 2 (February 16, 2023): 544. http://dx.doi.org/10.3390/v15020544.
Повний текст джерелаAndo, Wataru. "Polyorganosilicon Compounds in Strained Carbocyclic Systems." Bulletin of the Chemical Society of Japan 69, no. 1 (January 1996): 1–16. http://dx.doi.org/10.1246/bcsj.69.1.
Повний текст джерелаYavari, Issa, and Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds and Complexes Based on Acenaphthylene-1,2-dione." Synthesis 50, no. 20 (August 16, 2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.
Повний текст джерелаGaber, Hatem M., Mark C. Bagley, Zeinab A. Muhammad, and Sobhi M. Gomha. "Recent developments in chemical reactivity of N,N-dimethylenamino ketones as synthons for various heterocycles." RSC Advances 7, no. 24 (2017): 14562–610. http://dx.doi.org/10.1039/c7ra00683g.
Повний текст джерелаHalimehjani, Azim Ziyaei, Irishi N. N. Namboothiri, and Seyyed Emad Hooshmand. "Nitroalkenes in the synthesis of carbocyclic compounds." RSC Advances 4, no. 59 (June 24, 2014): 31261. http://dx.doi.org/10.1039/c4ra04069d.
Повний текст джерелаBartulewic, D., A. Markowska, S. Wołczyński, M. Dabrowska, and A. Rózański. "Molecular modelling, synthesis and antitumour activity of carbocyclic analogues of netropsin and distamycin--new carriers of alkylating elements." Acta Biochimica Polonica 47, no. 1 (March 31, 2000): 23–35. http://dx.doi.org/10.18388/abp.2000_4059.
Повний текст джерелаNiu, Ben, Yin Wei та Min Shi. "Recent advances in annulation reactions based on zwitterionic π-allyl palladium and propargyl palladium complexes". Organic Chemistry Frontiers 8, № 13 (2021): 3475–501. http://dx.doi.org/10.1039/d1qo00273b.
Повний текст джерелаLiu, Yuxiao, Yu Liu, Charles S. Shanahan, Xichen Xu, and Michael P. Doyle. "A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks." Org. Biomol. Chem. 12, no. 28 (2014): 5227–34. http://dx.doi.org/10.1039/c4ob00709c.
Повний текст джерелаMorikawa, Tetsuo. "Graph-Theoretical Enumeration of Conjugated Patterns for Carbocyclic and Heterocyclic Compounds*." Zeitschrift für Naturforschung A 49, no. 3 (March 1, 1994): 511–14. http://dx.doi.org/10.1515/zna-1994-0310.
Повний текст джерелаBanwell, MG. "New Methods for the Synthesis of Troponoid Compounds." Australian Journal of Chemistry 44, no. 1 (1991): 1. http://dx.doi.org/10.1071/ch9910001.
Повний текст джерелаZhang, Tao, Zi-Yu Zhang, Guowei Kang, Tao Sheng, Jie-Lun Yan, Yuan-Bin Yang, Yuxin Ouyang, and Jin-Quan Yu. "Enantioselective remote methylene C−H (hetero)arylation of cycloalkane carboxylic acids." Science 384, no. 6697 (May 17, 2024): 793–98. http://dx.doi.org/10.1126/science.ado1246.
Повний текст джерелаChen, Houguang Jeremy, Ronald Hong Xiang Teo, Jonathan Wong, Yongxin Li, Sumod A. Pullarkat та Pak-Hing Leung. "Challenges in cyclometalation: steric effects leading to competing pathways and η1,η2-cyclometalated iridium(iii) complexes". Dalton Transactions 47, № 37 (2018): 13046–51. http://dx.doi.org/10.1039/c8dt02639d.
Повний текст джерелаBarbera, J., E. Melendez, J. L. Serrano, M. T. Sierra, A. Ezcurra, and M. A. Perez Jubindo. "Chiral Mesogenic Compounds: Carbocyclic and Heterocyclic Schiff Bases." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 170, no. 1 (May 1989): 151–57. http://dx.doi.org/10.1080/00268948908047755.
Повний текст джерелаANDO, W. "ChemInform Abstract: Polyorganosilicon Compounds in Strained Carbocyclic Systems." ChemInform 27, no. 17 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199617312.
Повний текст джерелаAl Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups." Reactions 5, no. 2 (May 1, 2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Повний текст джерелаPućkowska, Anna, Krzysztof Bielawski, Anna Bielawska, and Andrzej Rózański. "New carbocyclic analogues of netropsin: synthesis and inhibition of topoisomerases." Acta Biochimica Polonica 49, no. 1 (March 31, 2002): 177–83. http://dx.doi.org/10.18388/abp.2002_3834.
Повний текст джерелаAndrés, Patricia, Gema Ballano, M. Isabel Calaza та Carlos Cativiela. "Synthesis of α-aminoboronic acids". Chemical Society Reviews 45, № 8 (2016): 2291–307. http://dx.doi.org/10.1039/c5cs00886g.
Повний текст джерелаDoraghi, Fatemeh, Mohammad Mahdi Aghanour Ashtiani, Fatemeh Moradkhani, Bagher Larijani та Mohammad Mahdavi. "Developments and applications of α-bromonitrostyrenes in organic syntheses". RSC Advances 14, № 21 (2024): 14835–46. http://dx.doi.org/10.1039/d4ra02474e.
Повний текст джерелаBattistini, Lucia, Claudio Curti, Gloria Rassu, Andrea Sartori, and Franca Zanardi. "Enolizable Alkylidene Heterocyclic and Carbocyclic Carbonyl Systems: Valuable Vinylogous Donor Substrates in Synthesis." Synthesis 49, no. 11 (April 6, 2017): 2297–336. http://dx.doi.org/10.1055/s-0036-1589487.
Повний текст джерелаErian, Ayman W., Yvette A. Issac, and Sherif M. Sherif. "A Novel Synthesis of Sulfone Systems as Antimicrobial Agents." Zeitschrift für Naturforschung B 55, no. 1 (January 1, 2000): 127–32. http://dx.doi.org/10.1515/znb-2000-0119.
Повний текст джерелаSivakrishna, Balija, Sehbanul Islam, Amarendra Panda, Maddi Saranya, Manas K. Santra, and Shantanu Pal. "Synthesis and Anticancer Properties of Novel Truncated Carbocyclic Nucleoside Analogues." Anti-Cancer Agents in Medicinal Chemistry 18, no. 10 (January 23, 2019): 1425–31. http://dx.doi.org/10.2174/1871520618666180322120533.
Повний текст джерелаLautens, Mark, Dino Alberico, Cyril Bressy, Yuan-Qing Fang, Brian Mariampillai, and Thorsten Wilhelm. "Palladium-catalyzed ring-forming reactions: Methods and applications." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 351–61. http://dx.doi.org/10.1351/pac200678020351.
Повний текст джерелаShinde, Madhuri V., Rohini S. Ople, Ekta Sangtani, Rajesh Gonnade, and D. Srinivasa Reddy. "Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction." Beilstein Journal of Organic Chemistry 11 (June 23, 2015): 1060–67. http://dx.doi.org/10.3762/bjoc.11.119.
Повний текст джерелаQuadrelli, Paolo, Naiara Vazquez Martinez, Roberto Scrocchi, Antonino Corsaro, and Venerando Pistarà. "Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol." Scientific World Journal 2014 (2014): 1–12. http://dx.doi.org/10.1155/2014/492178.
Повний текст джерелаZhou, Jian, Guannan Wang, Li-He Zhang, and Xin-Shan Ye. "From Exocyclic-Olefinic Carbohydrate Derivatives to Functionalized Carbocyclic Compounds." Current Organic Chemistry 10, no. 6 (April 1, 2006): 625–42. http://dx.doi.org/10.2174/138527206776359711.
Повний текст джерелаTADANO, Kin-ichi, and Tetsuo SUAMI. "Chiral synthesis of alkaloids and carbocyclic compounds from carbohydrates." Journal of Synthetic Organic Chemistry, Japan 44, no. 7 (1986): 633–46. http://dx.doi.org/10.5059/yukigoseikyokaishi.44.633.
Повний текст джерелаHalimehjani, Azim Ziyaei, Irishi N. N. Namboothiri, and Seyyed Emad Hooshmand. "ChemInform Abstract: Nitroalkenes in the Synthesis of Carbocyclic Compounds." ChemInform 45, no. 47 (November 6, 2014): no. http://dx.doi.org/10.1002/chin.201447261.
Повний текст джерелаSaborit, Gisela V., Carlos Cativiela, Ana I. Jiménez, Josep Bonjoch, and Ben Bradshaw. "Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation." Beilstein Journal of Organic Chemistry 14 (October 9, 2018): 2597–601. http://dx.doi.org/10.3762/bjoc.14.237.
Повний текст джерелаMorikawa, Tetsuo. "Structural Features for Non-Existence of Conjugated Patterns for Carbocyclic and Heterocyclic Compounds." Zeitschrift für Naturforschung A 49, no. 6 (June 1, 1994): 719–22. http://dx.doi.org/10.1515/zna-1994-0611.
Повний текст джерелаJiang, Yue-Ming, Jie Liu, Qiang Fu, Yu-Ming Yu, and Da-Gang Yu. "Visible-Light-Driven Phosphonoalkylation of Alkenes." Synlett 32, no. 04 (February 12, 2021): 378–82. http://dx.doi.org/10.1055/s-0040-1706681.
Повний текст джерелаArciszewska, Karolina, Anna Pućkowska, Agnieszka Wróbel, and Danuta Drozdowska. "Carbocyclic Analogues of Distamycin and Netropsin." Mini-Reviews in Medicinal Chemistry 19, no. 2 (December 6, 2018): 98–113. http://dx.doi.org/10.2174/1389557518666181009143203.
Повний текст джерелаLakeev, Sergei N., Irina O. Maydanova, Fanur Z. Galin, and Genrikh A. Tolstikov. "Sulfur ylides in the synthesis of heterocyclic and carbocyclic compounds." Russian Chemical Reviews 70, no. 8 (August 31, 2001): 655–72. http://dx.doi.org/10.1070/rc2001v070n08abeh000645.
Повний текст джерелаSavoia, Diego, Giuseppe Falini, and Andrea Gualandi. "Rhodium/Graphite-Catalyzed Hydrogenation of Carbocyclic and Heterocyclic Aromatic Compounds." Synthesis 2009, no. 14 (June 2, 2009): 2440–46. http://dx.doi.org/10.1055/s-0029-1216852.
Повний текст джерелаKeshavarz, Mohammad Hossein, and Hamid Reza Pouretedal. "New approach for predicting melting point of carbocyclic nitroaromatic compounds." Journal of Hazardous Materials 148, no. 3 (September 30, 2007): 592–98. http://dx.doi.org/10.1016/j.jhazmat.2007.03.014.
Повний текст джерелаMüllen, Klaus. "Book Review: Non-Benzenoid Conjugated Carbocyclic Compounds. By D. Lloyd." Angewandte Chemie International Edition in English 24, no. 11 (November 1985): 1007–8. http://dx.doi.org/10.1002/anie.198510072.
Повний текст джерелаMatyugina, E. S., S. N. Andreevskaya, T. G. Smirnova, and A. L. Khandazhinskaya. "Carbocyclic Analogues of Inosine-5’-Monophosphate: Synthesis and Biological Activity." Acta Naturae 4, no. 4 (December 15, 2012): 73–77. http://dx.doi.org/10.32607/20758251-2012-4-4-73-77.
Повний текст джерелаHronowski, Lucjan J. J., and Walter A. Szarek. "Synthesis of cyclopentane analogs of (2′- and 3′-deoxy-erythro-pentofuranosyl and ribofuranosyl)-2-thiouracil nucleosides." Canadian Journal of Chemistry 64, no. 8 (August 1, 1986): 1620–29. http://dx.doi.org/10.1139/v86-268.
Повний текст джерелаHronowski, Lucjan J. J., and Walter A. Szarek. "Synthesis of cyclopentane analogs of 5-fluorouracil nucleosides." Canadian Journal of Chemistry 70, no. 4 (April 1, 1992): 1162–69. http://dx.doi.org/10.1139/v92-152.
Повний текст джерелаKitamura, Masato, Kengo Miyata, Tomoaki Seki, Namdev Vatmurge, and Shinji Tanaka. "CpRu-catalyzed asymmetric dehydrative allylation." Pure and Applied Chemistry 85, no. 6 (April 15, 2013): 1121–32. http://dx.doi.org/10.1351/pac-con-12-10-02.
Повний текст джерелаDurakov, S. A., A. A. Kolobov, and V. R. Flid. "Features of heterogeneous catalytic transformations of strained carbocyclic compounds of the norbornene series." Fine Chemical Technologies 17, no. 4 (September 30, 2022): 275–97. http://dx.doi.org/10.32362/2410-6593-2022-17-4-275-297.
Повний текст джерелаYang, De-Suo, Zheng-Hui Guan, Sen Ke, Ming-Jin Fan, Hai-Tao Zhu, and Xiao-Ling Wang. "A Facile and Efficient Synthesis of Six-Membered Enol Carbocyclic Compounds." Synlett 26, no. 20 (October 28, 2015): 2826–30. http://dx.doi.org/10.1055/s-0035-1560517.
Повний текст джерелаGallos, John K., Zoe S. Massen, Theocharis V. Koftis, and Constantinos C. Dellios. "Carbocyclic nucleoside precursors by intramolecular cyclopropanation of sugar-derived diazo compounds." Tetrahedron Letters 42, no. 42 (October 2001): 7489–91. http://dx.doi.org/10.1016/s0040-4039(01)01556-8.
Повний текст джерелаGutke, Hans-Jürgen, and Dietrich Spitzner. "Resin-bound anionically induced Domino reactions; synthesis of functionalized carbocyclic compounds." Tetrahedron 55, no. 13 (March 1999): 3931–36. http://dx.doi.org/10.1016/s0040-4020(99)00113-1.
Повний текст джерелаMARUYAMA, Tokumi, and Mitsutoshi FUKUHARA. "Synthesis and Antitumor Activity of Phenyl Carbocyclic Oxetanocin and Related Compounds." CHEMICAL & PHARMACEUTICAL BULLETIN 44, no. 7 (1996): 1407–11. http://dx.doi.org/10.1248/cpb.44.1407.
Повний текст джерелаDOLGII, I. E., V. G. BORDAKOV, O. B. VETROVA, G. A. GRIGOR'EVA, E. A. KATSMAN, O. M. NEFEDOV, V. N. PAVLYCHEV, N. V. TRESHCHALINA, and T. A. BORTYAN. "ChemInform Abstract: Preparation of Carbocyclic Compounds and Synthesis on Their Basis." ChemInform 25, no. 25 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199425313.
Повний текст джерелаAl-Saad, Dalya, Misal Giuseppe Memeo, and Paolo Quadrelli. "#Nitrosocarbonyls 1: Antiviral Activity ofN-(4-Hydroxycyclohex-2-en-1-yl)quinoline-2-carboxamide against the Influenza A Virus H1N1." Scientific World Journal 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/472373.
Повний текст джерелаHanessian, Stephen, Daljit S. Dhanoa та Pierre L. Beaulieu. "Synthesis of carbocycles from ω-substituted α,β-unsaturated esters via radical-induced cyclizations". Canadian Journal of Chemistry 65, № 8 (1 серпня 1987): 1859–66. http://dx.doi.org/10.1139/v87-312.
Повний текст джерелаHalliday, Jill I., Mary Chebib, and Malcolm D. McLeod. "Synthesis and Biological Evaluation of a New Family of Constrained Azabicyclic Homocholine Analogues." Australian Journal of Chemistry 63, no. 5 (2010): 808. http://dx.doi.org/10.1071/ch10024.
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